Journal of the Chemical Society. Perkin transactions I p. 961 - 962 (1996)
Update date:2022-09-26
Topics:
Ohtani, Takehiko
Kikuchi, Keiichi
Kamezawa, Makoto
Hamatani, Hideaki
Tachibana, Hojun
Totani, Tetsuzo
Naoshima, Yoshinobu
An acetylenic alcohol, (+)-(4E, 15E)-docosa-4,15-dien-1-yn-3-ol 1, isolated from the marine sponge Cribrochalina vasculum, was synthesized in highly enantiomerically pure form by lipase-catalysed transesterification with Novozym 435 (Candida antarctica).
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